{
    "disease_id": "DOID:2235", 
    "synonyms": [
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013361", 
            "name": "congenital prothrombin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013361", 
            "name": "factor 2 deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013361", 
            "name": "Dysprothrombinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013361", 
            "name": "hereditary prothrombin deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013361", 
            "name": "hypoprothrombinemia"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013361", 
            "name": "factor II deficiency"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013361", 
            "name": "prothrombin deficiency, congenital"
        }, 
        {
            "url": "https://monarchinitiative.org/disease/MONDO:0013361", 
            "description": "", 
            "resource": "MONDO", 
            "id": "MONDO:0013361", 
            "name": "congenital factor II deficiency"
        }, 
        {
            "url": "http://disease-ontology.org/term/DOID:2235", 
            "description": "", 
            "resource": "Disease Ontology", 
            "id": "DOID:2235", 
            "name": "hypoprothrombinemia"
        }
    ], 
    "recommended_name": {
        "url": "http://disease-ontology.org/term/DOID:2235", 
        "description": "A thrombophilia that is characterized by bleeding symptoms due to low levels of circulating prothrombin, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the gene encoding coagulation factor II, also known as prothrombin, on chromosome 11p11.", 
        "resource": "Disease Ontology", 
        "id": "DOID:2235", 
        "name": "prothrombin deficiency"
    }, 
    "evidence": [
        {
            "url": "https://www.alliancegenome.org/gene/2235#disease-associations", 
            "id": "2235", 
            "database": "Alliance of Genome Resources"
        }
    ]
}